Harlequin fetus

Preferred Label : Harlequin fetus;

Rare : true;

Source : OMS;

Date de début : 01/01/1997;

Origin ID

Q804;

UMLS CUI

C0239849;

Automatic exact mappings (from CISMeF team)
- ichthyosis, lamellar [MeSH Descriptor]
Currated CISMeF NLP mapping
- Harlequin Ichthyosis [NCIt concept]
- Harlequin fetus [MedDRA LLT]
- Harlequin fetus [PASCAL descriptor]
- Harlequin fetus [ICD-10 Sub-category (who)]
- Harlequin fetus (disorder) [SNOMED CT concept]
- Harlequin foetus [MedDRA Preferred Term]
- Harlequin ichthyosis [Disease (Nov.)]
- Harlequin ichthyosis [ORDO Disease]
- Harlequin ichthyosis [ICD-11 More detail]
- Harlequin ichthyosis (disorder) [SNOMED CT concept]
- Harlequin type ichthyosis [MeSH concept]
- Ichthyosis, congenital, autosomal recessive 4b [OMIM Phenotype]
- harlequin fetus [MeSH concept]
- harlequin fetus [SNOMED Notion]
- harlequin type ichthyosis [MeSH Supplementary Concept]
DO Cross reference
- autosomal recessive congenital ichthyosis 4B [DO Concept]
Orphanet concepts
- Harlequin ichthyosis [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Harlequin Ichthyosis [NCIt concept]
- Harlequin fetus [MedDRA LLT]
- Harlequin fetus [PASCAL descriptor]
- Harlequin fetus (disorder) [SNOMED CT concept]
- Harlequin foetus [MedDRA Preferred Term]
- Harlequin ichthyosis (disorder) [SNOMED CT concept]
- harlequin fetus [MeSH concept]
- harlequin fetus [SNOMED Notion]